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B. D. Einerson and A. P. Soisson
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the International Society for Abnormally Invasive Placenta. Am J Obstet Gynecol. 2019;220(6):511–26.
39. Scaglione MA, Allshouse AA, Caneld DR, et al. Prophylactic ureteral stent placement and urinary injury during hysterectomy for placenta accreta spec­trum. Obstet Gynecol. 2022;140(5):806–11.

Inguinal Lymphadenectomy, Radical Vulvectomy

ClarissaLam andMarioM.Leitao
31
Background ofLymphedema After Inguinofemoral Lymphadenectomy
Lower extremity lymphedema (LEL) is a rela­tively common complication of inguinofemoral lymphadenectomy (IFL). Rates of LEL after IFL in patients with melanoma have been reported between 13% and 55% [1]. Lymphedema can either be a temporary or a chronic and debilitat­ing condition. In one series of 204 patients with melanoma, 58 patients underwent IFL and 26% of patients had measurable LEL six months post­operatively, with 8% of patients having signi­cant functional decits [104]. In the GROINSS-V-1 prospective trial, the rate of LEL was 25.2% after sentinel lymph node (SLN) dis­section with lymphadenectomy versus 1.9% after SLN dissection alone [105].
Vulvectomy and IFL are typically performed
using separate incisions. In one study, approxi-
C. Lam Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA e-mail: LamC2@mskcc.org
M. M. Leitao (*) Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA
Department of Obstetrics and Gynecology, Weill Cornell Medical College, New York, NY, USA e-mail: leitaom@mskcc.org
mately three-quarters of patients who underwent modied radical vulvectomy and inguinal lymph­adenectomy with separate incisions had one or more documented complications, with 28% of patients experiencing lymphedema [33]. The next sections will cover methods identied in the literature to recognize, prevent, and manage lymphedema.
Recognition ofLymphedema Following Inguinofemoral Lymphadenectomy
Radionuclide lymphoscintigraphy is the gold standard imaging modality for the diagnosis of lymphedema; it is also useful in surgical plan­ning. Other imaging modalities include mag­netic resonance lymphangiography and indocyanine green lymphangiography. Medical history and physical examination by qualied health care practitioners, however, have been used to accurately diagnose patients in approxi­mately 90% of cases [39]. Secondary lymph­edema after lymphadenectomy typically presents 12 to 18 months after the inciting injury. Lymphedema almost universally involves the distal extremity and leads to pitting edema on examination. Grading and/or staging can be performed for lymphedema (Table 31.1, Fig. 31.1). Lymphedema after IFL, however, can manifest in the upper thigh, vulva, and/or
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2025 M. Hoffman et al. (eds.), Major Complications of Female Pelvic Surgery,
https://doi.org/10.1007/978-3-031-66772-5_31
333
334
cd
Table 31.1 Grading systems for lymphedema (Dessources et al. 2020)
ISL stage ISL grading CTCAE grade 0: Subclinical impaired lymphatic transport
without lymphedema 1: Relatively high protein edema that
reverses with elevation +/− pitting +/− increase in proliferating cells
2: High protein edema with dermal brosis that does not easily reverse with elevation. Usually no pitting
3: Trophic skin changes: warty overgrowths, acanthosis, fat deposits, usually without pitting. Also known as lymphatic elephantiasis
ISL International Society of Lymphology, CTCAE Common Terminology Criteria for Adverse Events
Mild, <20% increase in volume
Moderate, 20%–40% increase in volume
Severe, >40% increase in size Grade 3: Severe symptoms
Grade 1: Trace thickening or faint skin discoloration
Grade 2: Limits activities of daily living. Characterized by marked skin discoloration, leathery texture, and papillary formation
limiting self-care and activities of daily living
C. Lam and M. M. Leitao
ab
Mild Stage 1
Moderate Stage 1Moderate Stage 2Severe Stage 3
Fig. 31.1 International Society of Lymphology stages/ grade of lymphedema. (a) Stage 1 mild lymphedema with 40% limb difference, and abnormal fat deposits; (b) Stage 1 moderate lymphedema with a 20%–40% differ­ence in limb size; (c) Stage 2 moderate lymphedema with
mons pubis. The Stemmer sign, or the inability to pinch up the skin on the dorsum of the foot, is also a sensitive and specic sign of lymph­edema. The presence of these factors in the his­tory and on physical examination can help rule out other diagnoses such as a venous thrombo­embolic event, heart failure, renal failure, or venous insufciency. Of note, adult-onset pri­mary lymphedema is rare. Lymphedema is a chronic condition that progresses through four stages and can be assessed on physical examina­tion [53].
a 20%–40% difference in limb size with associated bro­sis and irreversible edema; (d) Stage 3 severe lymph­edema with >40% limb difference, and abnormal fat deposits (Dessources etal. 2020)
Prevention ofLymphedema Following Inguinofemoral Lymphadenectomy
Some data suggest there is no benet to the rou­tine prescription of graduated compression stock­ings in the prevention of lymphedema after IFL [100]. Findings from other studies, however, sug­gest that the use of compression stockings com­bined with patient education delays the onset or even reduces the risk of lymphedema [47, 95].
31 Inguinal Lymphadenectomy, Radical Vulvectomy
335
A historical study of interest that randomized patients with vulvar cancer with positive nodes after radical vulvectomy and IFL to either adju­vant radiation therapy or pelvic lymph node dis­section found that adjuvant radiation therapy was associated with a decreased risk of lymphedema and improved two-year survival rates [51]. On the topic of radiotherapy, adjuvant radiation after IFL increases the risk of lymphedema by way of decreased lymphatic proliferation potential, interstitial brosis compressing lymphatic ves­sels, and precipitating mechanical insufciency of the lymphatic system [4]. Thus, avoiding adju­vant radiation unless clearly clinically indicated can help prevent LEL. To decrease the use of unnecessary pelvic radiation, one study demon­strated that performing minimally invasive pelvic lymphadenectomy was an effective method to screen for patients who do not need adjuvant whole pelvic radiation after IFL [58].
Whenever feasible and indicated, SLN dis­section without full IFL is the best method to prevent lower extremity edema. In general, the indication for lymph node sampling includes any tumor greater than stage IA.Omitting full IFL is reasonable in vulvar tumors <4cm. Full lymphadenectomy after SLN dissection depends on the size of the SLN metastases. In the GROINSS-V-I study, 135 patients with positive SLNs were identied; 115 underwent IFL with a 6% groin recurrence rate, 14 underwent radia­tion therapy with a 14% groin recurrence rate, and 4 had no treatment with a 25% groin recur­rence rate. Omitting IFL in patients with nega­tive SLNs was found to be safe and was associated with a decreased rate of LEL (1.9% with SLN sampling alone versus 25.2% with SLN sampling and IFL, P < 0.0001) [105]. GROINSS-V-II, a subsequent prospective phase II trial examining radiation therapy in patients with positive SLNs without IFL, found the risk of groin recurrence was signicantly lower in patients with an SLN metastasis 2 mm (P=0.008). This study also found signicantly lower rates of lymphedma in the radiotherapy­only group compared to patients who had IFL with or without adjuvant radiation therapy [72]. Patients who underwent IFL had lymphedema
rates of 32% and 22.9% at 6 months and 12months, respectively.
Saphenous vein preservation has been shown to be associated with less morbidity. A meta­analysis of four studies demonstrated that preser­vation of the saphenous vein was associated with a decreased risk of LEL (OR: 0.24, 95% CI:
0.11–0.53), wound necrosis (OR: 0.34, 95% CI:
0.19–0.59), and acute cellulitis (OR: 0.4, 95% CI: 0.16–0.96) [1]. In a retrospective evaluation of patients with vulvar squamous cell carcinoma who underwent IFL, saphenous vein preservation was associated with reduced risk of wound cel­lulitis, wound breakdown, and chronic lymph­edema [23]. A systematic literature review of 36 studies on IFL morbidity found that sparing the saphenous vein decreased wound infections, wound breakdown, cellulitis/erysipelas, and lymphedema (Table31.2) [23, 81, 87, 110, 25].
Preservation of the fascia lata of the major anterior thigh muscles of the femoral triangle during IFL has also been associated with a decreased risk of postoperative LEL. The pro­posed mechanism for this association is the maintenance of the unidirectional valves of the veins and lymphatics [40, 109]. In one study investigating this fascia-preserving technique, the researchers made a curvilinear incision at the base of the femoral triangle, creating a ap between the supercial and deep layers of the Camper’s fascia. At the completion of nodal dis­section, the ap was sutured to the fascia lata to eliminate dead space [109]. With this technique, the authors noted a 12% rate of lymphedema. Skin necrosis and local infection made up 5.5% and 2.5% of the postoperative complications in this study, respectively, and oncological out­comes were not compromised.
Pedicled omentoplasty is another technique to decrease the risk of LEL after IFL. This tech­nique, which has been reported after pelvic lymph node dissections, is thought to decrease LEL by altering the absorption or transport of lymph uids. The benet of pedicled omento­plasty in IFL was tested in a pilot study of four women and three men with inguinal metastatic lymph nodes [11]. After IFL, four of the seven patients had mild asymptomatic lymphedema,
336
Overall 1
complication
C. Lam and M. M. Leitao
Short term Long term
Wound infection Wound breakdown Lymphocele Lymphedema Cellulitis/erysipelas
Table 31.2 Summary of rates of short-term and long-term complications separated by saphenous vein sparing and saphenous vein ligating techniques [81]
Study N Sparing Ligation P-value Sparing Ligation P-value Sparing Ligation P-value Sparing Ligation P-value Sparing Ligation P-value
49 0 45 <0.001 0 25 <0.02 0 0 11 39 <0.05 0 6 NS
Per groin
Dardarian
2006
355 18 30 0.01 16 36 <0.001 – 23 45 <0.001 –
Rouzier
2003
139 – 13 38 0.001 10 4 NS 32 70 18 39 0.006
Zhang
2000
128 68 73 NS 26 32 NS 25 48 <0.01 21 41 <0.05
Zhang
2007
31 Inguinal Lymphadenectomy, Radical Vulvectomy
337
and the remaining three, who were noted to have lymphedema preoperatively, had improvement in their symptoms postoperatively. To achieve this ap, surgeons in this study made both an abdomi­nal and an inguinal incision, mobilized an omen­tal ap, passed the ap deep to the inguinal ligament through the femoral canal, and sutured it into place. In this study, the saphenous vein was ligated at its proximal and distal ends. One dif­culty that surgeons encountered with this tech­nique was the inadequate length of the omental ap. This technique has yet to be validated in larger trials. Omental nodal harvest can also be achieved via a free-ap method, which does not require passage through the femoral canal and eliminates concern about adequate length; how­ever, it would require an adequately vascularized ap with microsurgical anastomosis to vessels in the groin [11].
Lymphovenous anastomosis (LVA) is another technique to help prevent the development of LEL.This approach involves simultaneously pre­paring an accessory branch of the femoral vein at the time of lymphadenectomy of the groin (or axillary vein in the case of axillary lymph node dissection) followed by an anastomosis with one or more afferent lymphatic vessels (Fig. 31.2). Jørgensen et al. conducted a systematic meta­analysis of studies treating patients with prophy­lactic LVA following lymphadenectomy to prevent lymphedema. In a quantitative analysis of studies including a control group, the authors found patients treated with prophylactic LVA had
Fig. 31.2 Lymphovenous anastomosis. (Courtesy of Dr. Mario M.Leitao, Jr.)
a relative risk of 0.33 (95% CI: 0.19–0.56) for developing lymphedema compared to controls [56]. Of note, ve of these studies involved patients with gynecologic cancer, two of which involved patients with vulvar cancer specically. Morotti et al. performed one of the two studies and assessed microsurgical LVA in the prevention of lymphedema in patients with vulvar cancer. This study demonstrated the feasibility of LVA at the time of IFL.LVA appears to be a promising technique for decreasing lymphedema in high­risk patients, although more studies are needed.
Laparoendoscopic single-site surgery (LESS) is a minimally invasive technique that has recently been used for IFL in gynecologic oncol­ogy diseases, including vulvar and vaginal can­cers. A small single-site study, which evaluated six patients with vulvar or vaginal cancer who underwent LESS for inguinal lymphadenectomy from July 2018 to March 2019, demonstrated LESS is a feasible and safe technique for the management of these gynecologic malignancies, with no reported postoperative complications [108]. However, this is an extremely small series to make denitive recommendations.
Robotic-assisted video endoscopic inguinal lymphadenectomy (RAVEIL) is another mini­mally invasive technique used for IFL.The feasi­bility of this modality was demonstrated in a study by Josephson etal. [57]. In a retrospective study, reduced complication rates were noted with RAVEIL for the management of penile carcinoma compared with an open approach, while maintain­ing adequate surgical outcomes [89]. In this study, saphenous vein preservation was more likely with RAVEIL compared to standard- approach inguinal lymphadenectomy. Video endoscopic inguinal lymphadenectomy (VEIL) without robotic assis­tance was studied in 46 patients with vulvar can­cer, and VEIL was associated with reduced postoperative complications compared to tradi­tional open technique for inguinal lymphadenec­tomy [64]. Therefore, the use of VEIL by trained surgeons, with or without robotic assistance, may be considered in patients with vulvar cancer to decrease the risk of postoperative complications. This approach, however, requires more investiga­tion before routine adoption.
338
Management ofLymphedema Following Inguinofemoral Lymphadenectomy
Conservative options for the management of lymphedema include lower extremity elevation when at rest, compression techniques, manual lymphatic drainage, exercise, intermittent pneu­matic compression devices, and low-level laser therapy. There are no clear data to suggest which, if any, of these measures is most effective in the treatment of lymphedema; although, there does not seem to be any harm documented as a result of these treatments [73].
Surgical management of lymphedema includes two approaches: physiologic and abla­tive. Physiologic surgical options attempt to improve lymph ow by supporting lymphatic pathways, whereas ablative surgical options aim to debulk lymphedematous areas and reduce morbidity [60]. Lymphaticovenular anastomo­sis, also known as lymphovenous bypass, is a physiologic surgical technique to reroute lym­phatic uid into the venous system; however, there are mixed data regarding the efcacy of this technique (Fig. 31.3) [18, 22, 32, 52, 59]. Vascularized lymph node transfer is the pre­ferred modality to restore lymphatic drainage in dysfunctional lymph node basins after lymphad­enectomy or radiation therapy. This technique entails the transfer of vascularized lymph nodes to the desired area either via free aps or in a pedicled fashion. Although there is a rare risk of iatrogenic lymphedema due to lymphatic disrup­tion at the transfer site [78, 101, 106, 107], most studies have demonstrated improvement in lymphedema symptoms and quality of life [19,
66, 74, 83]. For advanced-stage chronic lymph-
edema, ablative procedures such as the Charles procedure, which involves the removal of skin and subcutaneous tissue followed by skin grafts, may restore functional decits and provide relief in debilitating lymphedema. Suction-assisted lipectomy can be useful in patients who do not have signicant pitting edema and who are not candidates for other surgical techniques. Although this method is limited, good patient satisfaction has been reported with suction­assisted lipectomy [13, 14].
C. Lam and M. M. Leitao
Fig. 31.3 Lymphovenous bypass. (Courtesy of Dr. Mario M.Leitao, Jr.)
Background ofInfectious Morbidity Following Radical Vulvectomy andInguinofemoral Lymphadenectomy
Vulvectomy has long been known to have high rates of postoperative complications due to sev­eral host factors, including the specic microbial ora of the genital tract and its surrounding struc­tures, decreased host immunity due to malig­nancy and other potential comorbidities, prior chemotherapy or radiation in the area, and dif­culty of wound care at the surgery site. One study noted a wound infection rate of 7%, and the most common pathogens isolated from wound sites were Pseudomonas aeruginosa, Enterococcus, and Escherichia coli [29].
Although SLN mapping is now an accepted standard for vulvar cancer staging, there are still instances when full IFL is warranted, particularly in patients with vulvar tumors 4cm or multifo-
31 Inguinal Lymphadenectomy, Radical Vulvectomy
339
cal disease. IFL performed for the purpose of sampling enlarged groin lymph nodes is associ­ated with a complication rate as high as 60% [40,
98], with the most common complications being
lymphorrea, seroma, infection, and wound break­down. Some suggested predictors of postopera­tive complications include number of lymph nodes removed, pathologically positive nodes, patient age, and disease stage [36]. Groin dissection is associated with a high risk of infec­tion due to the inherent moisture in the area and the risk of contamination. Rates of wound infec­tion after groin surgery range from 6% to 29% [10]. Wound infection invariably increases the risk of wound breakdown. Gaarenstroom et al. [33] examined modied radical vulvectomy with IFL through separate incisions and found the incidence of wound breakdown was up to 39%, with or without infection [33]. The next sections will cover methods identied in the literature to recognize, prevent, and manage the complica­tions of wound infection.
Recognition ofInfectious Morbidity Following Radical Vulvectomy andInguinofemoral Lymphadenectomy
Clinical signs of infection, including leukocyto­sis and fever, should be used in conjunction with physical examination ndings including ery­thema, edema/induration, and/or purulent dis­charge. Wound breakdown can also be present. Necrotizing infection, which will usually present with pain out of proportion to physical examina­tion ndings, crepitus on palpation, skin discol­oration, and imaging ndings suggestive of gas in the area of interest, is important to rule out.
Prevention ofInfectious Morbidity Following Radical Vulvectomy andInguinofemoral Lymphadenectomy
As mentioned previously, the GROINSS-V-I study demonstrated a signicantly decreased risk of postoperative morbidity with SLN sampling
alone versus SLN sampling with IFL, with rates of wound breakdown of 11.7% versus 34.0%, respectively (P< 0.0001), and rates of cellulitis of 4.5% versus 21.3%, respectively (P<0.0001) [105].
Preoperative preparation of the skin and vagina with povidine-iodine or chlorhexidine gluconate is universally recommended to prevent infection [5], and should be performed for patients who undergo radical vulvectomy and/or IFL. A randomized controlled trial comparing the use of chlorhexidine gluconate and iodine for vaginal preparation prior to hysterectomy in 85 patients demonstrated decreased vaginal bacteria count in patients who underwent chlorhexidine preparation; although, no surgical site infections were identied in either group [46]. In a propen­sity score-matched analysis, however, povidine­iodine was shown to be preferable to chlorhexidine in vaginal preparation before hysterectomy due to lower rates of infection and fewer emergency department visits [97]. Thus, the choice of prepa­ration solution can be left to the surgeon’s prefer­ence due to the limited data supporting one over the other.
Aside from open versus endoscopic modali­ties, there is clear variation in actual surgical technique for groin surgery. One randomized controlled trial compared postoperative compli­cation rate with the use of LigaSure technology versus conventional (sharp/diathermia) technique and found the estimated incidence of 1 postop­erative complications was 29% after LigaSure versus 70% after conventional inguinal lymphad­enectomy (P < 0.001) [80]. Creating separate incisions for radical vulvectomy and lymphade­nectomy has been shown to decrease risk of infectious morbidity in several studies [29, 41].
The use of groin drains has been investigated in several studies. One retrospective cohort study by Pontre etal. showed the use of groin drains signicantly reduced the incidence of postopera­tive groin cellulitis (8.7% versus 25.4%, P=0.039) [79]. Duration of drain use does not seem to have an effect on the development of postoperative complications [37]. In a Dutch nationwide prospective study by Pouwer etal., using volume-based standards for drain removal was found to be superior to time-based removal
340
C. Lam and M. M. Leitao
(removal of drain on postoperative day ve) in decreasing complication rates (46% versus 75%, respectively, P = 0.006) [82]. Of note, no ran­domized controlled trials have compared surgical outcomes of inguinal lymphadenectomy with and without use of drains.
In a prospective clinical study examining post­operative outcomes after radical lymphadenec­tomy or SLN procedure, Asciutto etal. employed negative pressure wound therapy (NPWT) in con­junction with groin drains [6]. Surgical site com­plications were identied in 11 of the 20 patients (55%) who underwent NPWT; one patient suf­fered a wound rupture, six patients developed lymphoceles, and four patients had a surgical site infection. Although no statistical tests were per­formed, the use of NPWT in this small cohort was thought to reduce the severity of surgical site complications after inguinal lymphadenectomy. The efcacy of NPWT was evaluated in a meta­analysis of studies looking at its use in various other surgery types (orthopedic, abdominal, colorectal, and obstetric) and was associated with a signicant reduction in surgical site infection, wound dehiscence, and length of stay [99].
Modest weight loss preoperatively can poten­tially decrease the risk of development of at least one complication. In a study of 204 patients with melanoma, the risk of developing at least one complication for all patients who underwent regional lymph node dissection of the neck, axilla, and groin was increased in obese patients (P=0.05) [104].
It is common to recommend frequent sitz baths or loose-tting underwear postoperatively, but there are limited data to support these practices for the prevention of infection and wound break­down after vulvectomy in patients with gyneco­logic cancer. One randomized controlled trial examining sitz baths after episiotomy did not nd a statistically signicant decrease in the rate of wound breakdown [70]. Prospective data are still needed to optimize postoperative vulvar hygiene and wound care regimens in patients with gyneco­logic cancers. In addition to the above measures, some clinicians prescribe sitting restrictions to prevent direct pressure on the incisional area for four to six weeks postoperatively. Inatable
donut-like devices or soft pillows provide support and maintain quality of life for patients while fol­lowing sitting restrictions during recovery. However, no data are available that specically address the efcacy of sitting restrictions in pre­venting wound complications after vulvectomy.
Management ofInfectious Morbidity Following Radical Vulvectomy andInguinofemoral Lymphadenectomy
Infection should be managed with antibiotics, either parenteral or oral, and the antibiotic regi­men should be tailored based on the clinician’s judgement of infection severity. Wound culture should be obtained if applicable to the clinical scenario. Antibiotics should be started empiri­cally and tailored to wound culture results if obtained. In the setting of infection, there may be clinical utility to reopen the incision if the wound has not already opened on its own. The incision should then be allowed to close by secondary intention, whether with wet-to-dry dressing or NPWT, whichever is feasible. NPWT has the benet of evacuating wound uid, stimulating granulation tissue formation, and decreasing bac­terial colonization of the wound; although, in one retrospective study of the use of vacuum-assisted closure in complex wound failures, patients with gynecologic cancer complained of pain with wound dressing changes [94]. In this study, 96% of patients had complete wound healing. Extensive surgical debridement is the mainstay of treatment for necrotizing soft-tissue infections of the vulva [21]. If this is suspected, early and aggressive surgical resection is critical to mini­mizing morbidity and mortality.
Background ofFunctional Impairments After Radical Vulvectomy
Vulvectomy has the potential to result in sig­nicant anatomic distortion, leading to a num­ber of functional impairments, including
31 Inguinal Lymphadenectomy, Radical Vulvectomy
341
difculties with micturition, defecation, and sexual activity [48].
In one questionnaire study, fecal incontinence was reported in 43% of survivors of gynecologic cancer [90]; however, rates of fecal incontinence in patients who underwent vulvectomy speci­cally were not reported.
Various forms of sexual dysfunction have been reported after a vulvectomy, including sex­ual aversion disorder, hypoactive sexual disorder, and arousal disorder. Factors associated with posttreatment sexual dysfunction in patients who underwent surgical treatment for vulvar cancer include increased age, poor overall well-being, history of depression or anxiety, and excision size of vulvar malignancy [2]. Compared to healthy controls, patients with vulvar cancer are at increased risk for sexual dysfunction, both before and after surgical excision [3]. Extent of surgery or type of vulvectomy has not been found to be correlated with the degree of sexual dys­function present postoperatively [38].
Pelvic Organ Prolapse Quantication system (POP-Q) to assess for pelvic organ prolapse con­tributing to urinary symptoms. Urinary tract infection should be ruled out in patients present­ing with new-onset urinary incontinence postop­eratively. Anatomic distortions, particularly in patients who underwent urethrectomy as part of radical vulvar surgery, can be identied on physi­cal examination as contributing factors to urinary incontinence; these patients can present with total incontinence (Fig.31.4).
When a patient presents with sexual dysfunc­tion, it is important to screen for psychosocial factors that may be contributing factors, includ­ing depression and relational discord. Physical examination can elucidate whether there is an anatomical aberration related to vulvar surgery, including introital stenosis or clitoral distortion (Fig.31.4).
Once again, performing a thorough history and physical examination are crucial to diagnos­ing fecal incontinence. Fistula can be an etiology
Recognition ofFunctional Impairments After Radical Vulvectomy
Functional impairments can be diagnosed based on patient-reported symptoms postoperatively. These symptoms can present immediately or even one year after primary surgery. According to a questionnaire-based study, only 40% of survi­vors of gynecologic cancer reported having been asked about urinary/fecal incontinence or sexual function by their oncologist [90], which high­lights the importance of obtaining a thorough his­tory and physical examination to recognize and treat these functional impairments.
Urinary incontinence is very common in post­menopausal patients, with or without radical vul­vectomy. Urinary incontinence should be separated by type, namely, urge, stress, or mixed incontinence. Because treatment will depend on the type of incontinence present, it is important to take a thorough history and perform a detailed physical examination, including specic tests such as the Q-tip test for urethral mobility and the
Fig. 31.4 Introital stenosis with urethral hooding and fecal incontinence after radical vulvectomy. (Courtesy of Dr. Mitchel Hoffman)